GB746692A - Improvements in or relating to interpolymers - Google Patents

Improvements in or relating to interpolymers

Info

Publication number
GB746692A
GB746692A GB3307/54A GB330754A GB746692A GB 746692 A GB746692 A GB 746692A GB 3307/54 A GB3307/54 A GB 3307/54A GB 330754 A GB330754 A GB 330754A GB 746692 A GB746692 A GB 746692A
Authority
GB
United Kingdom
Prior art keywords
interpolymer
methyl
natural rubber
specified
chloride
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB3307/54A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Goodrich Corp
Original Assignee
BF Goodrich Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BF Goodrich Corp filed Critical BF Goodrich Corp
Publication of GB746692A publication Critical patent/GB746692A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/18Introducing halogen atoms or halogen-containing groups
    • C08F8/20Halogenation
    • C08F8/22Halogenation by reaction with free halogens

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

An unsaturated partially halogenated interpolymer containing 1 to 5 per cent of iodine and chlorine is made by reacting with iodine monochloride at below 25 DEG C., preferably below 0 DEG C., an interpolymer comprising a major proportion of an iso-olefin containing from 4 to 8 carbon atoms and a terminal methylene group with a minor proportion of at least one polyolefinic hydrocarbon. A third monomer such as styrene, chlorostyrene, acrylyl chloride or methallyl chloride may be present in the interpolymer. Specified iso-olefins are isobutylene, 3-methyl or 2-ethyl butene-1, and 4-methyl- or -ethylpentene-1, while specified polyolefins include butadiene, isoprene, 2,4-dimethyl butadiene, piperylene, 2-methyl-hexadiene-1,5, cyclopentadiene, dipentane, sylvestrene, phellandrene, 2,6-dimethyl-4-methylene-heptadiene-2,5, myrcene, fulvene, 6-ethyl fulvene, 1,3,3-trimethyl-6-vinyl-cyclohexadiene-2,4, 6,6-vinyl-methyl-fulvene, phenyl butadienes, divinyl benzene, diallyl benzene and divinyl naphthalenes, many other similar compounds being specified. The halogenation may be effected by using a solution, dispersion or cement of the interpolymer and iodine parachloride in an organic solvent or diluent such as a hydrocarbon or halogen derivative thereof, e.g. methyl chloride. The product may be compounded with the usual vulcanizing ingredients and cured. It may also be mixed with natural rubber, polychloroprene, polybutadiene, copolymers of chloroprene, butadiene or isoprene with each other or with styrene, acrylonitrile, acrylic and methacrylic acids and their alkyl esters, vinyl pyridine and vinylidene chloride. Adhesive cements may be made from the interpolymer, channel black and heptane.ALSO:Natural rubber is mixed with vulcanizing agents (sulphur, mono and diheptyl diphenylamines, furnace black, zinc oxide, stearic acid, mercaptobenzothiazole, diortho-tolyl quanidine and sulphur are specified) and an isoolefin-polyolefin interpolymer which has been after-treated with iodine monochloride (see Group IV(a)) and cured. 30 parts natural rubber to 70 of interpolymer are used. The after-treated interpolymer may be mixed with channel black and n-heptane and used to bound together sheets of butyl type rubbers and natural rubber.
GB3307/54A 1953-03-02 1954-02-04 Improvements in or relating to interpolymers Expired GB746692A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US746692XA 1953-03-02 1953-03-02

Publications (1)

Publication Number Publication Date
GB746692A true GB746692A (en) 1956-03-21

Family

ID=22120929

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3307/54A Expired GB746692A (en) 1953-03-02 1954-02-04 Improvements in or relating to interpolymers

Country Status (3)

Country Link
DE (1) DE1033416B (en)
FR (1) FR1099182A (en)
GB (1) GB746692A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3085074A (en) * 1959-11-16 1963-04-09 Burke Aqueous dispersions of halogenated, polymer modified butyl rubber, process of makingsame, and vulcanization thereof
WO1991013102A1 (en) * 1990-03-01 1991-09-05 Exxon Chemical Patents Inc. Halogenation of polymers with improved neutralization
WO1993006138A1 (en) * 1991-09-17 1993-04-01 Exxon Chemical Patents Inc. Halogenation of star-branched butyl rubber with improved neutralization

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3085074A (en) * 1959-11-16 1963-04-09 Burke Aqueous dispersions of halogenated, polymer modified butyl rubber, process of makingsame, and vulcanization thereof
WO1991013102A1 (en) * 1990-03-01 1991-09-05 Exxon Chemical Patents Inc. Halogenation of polymers with improved neutralization
US5077345A (en) * 1990-03-01 1991-12-31 Exxon Chemical Patents Inc. Halogenation of polymers with improved neutralization
WO1993006138A1 (en) * 1991-09-17 1993-04-01 Exxon Chemical Patents Inc. Halogenation of star-branched butyl rubber with improved neutralization
US5286804A (en) * 1991-09-17 1994-02-15 Exxon Chemical Patents Inc. Halogenation of star-branched butyl rubber with improved neutralization

Also Published As

Publication number Publication date
DE1033416B (en) 1958-07-03
FR1099182A (en) 1955-08-31

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